Canonical Allele Identifier: CA2190338348

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80172038A= , CM000677.2:g.80172038A=	GRCh38
NC_000015.9:g.80464380A= , CM000677.1:g.80464380A=	GRCh37
NC_000015.8:g.78251435A=	NCBI36
NG_012833.1:g.24040A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.796-976A=
ENST00000561421.6:c.607-111A= MANE Select	ENSP00000453347.2:n.607-111A=
ENST00000646551.1:n.2234-124A=
ENST00000261755.9:c.607-111A=	ENSP00000261755.5:n.607-111A=
ENST00000407106.5:c.607-111A=	ENSP00000385080.1:n.607-111A=
ENST00000539156.5:c.397-111A=	ENSP00000454271.1:n.397-111A=
ENST00000558627.1:n.535-111A=
ENST00000561421.5:c.607-111A=	ENSP00000453347.1:n.607-111A=
NM_000137.2:c.607-111A=	NP_000128.1:n.607-111A=
XM_024449872.1:c.607-111A=	XP_024305640.1:n.607-111A=
NM_000137.4:c.607-111A= MANE Select	NP_000128.1:n.607-111A=
NM_001374377.1:c.607-111A=	NP_001361306.1:n.607-111A=
NM_001374380.1:c.607-111A=	NP_001361309.1:n.607-111A=